http://rdf.ncbi.nlm.nih.gov/pubchem/patent/IE-41516-L
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_966a6c1f382ec9bcb5e3839dfd73e5b8 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C43-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N31-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C41-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C43-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C43-00 |
| filingDate | 1975-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1976-02-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | IE-41516-L |
| titleOfInvention | Propargy lether insecticides |
| abstract | 1472839 Propargyl ethers F HOFFMANNLA ROCHE & CO AG 29 Aug 1975 [30 Aug 1974] 35742/75 Heading C2C The invention comprises compounds of formula where n is an integer of 8-12. These compounds may be prepared by reacting a compound X-(CH 2 ) n -X<SP>1</SP>, where X and X<SP>1</SP> each represent a chlorine, bromine or iodine atom or a mesyloxy or tosyloxy group, with at least two moles of an alcoholate MOCH 2 C#CH, where M is an alkali metal or alkaline earth metal, or by reacting a compound MO(CH 2 ) n OM with a compound XCH 2 C#CH. The alcoholate may be formed in situ from the alcohol and the metal or a hydride, amide or hydroxide of the metal. An inert organic solvent, e.g. dimethylformamide, dioxane, hexamethylphosphoric acid triamide, tetrahydrofuran or dimethoxyethane, is used for these reactions. The compounds are insecticides.n[GB1472839A] |
| priorityDate | 1974-08-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 39.